Canonical Allele Identifier: PA658807829
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 530522
ClinVar RCV Id: RCV001471060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asn534Ser
CA6571285
NM_014191.4:c.1601A>G